Detalhe da pesquisa
1.
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies.
Hum Genet
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38753158
2.
Lack of ApoA-I in ApoEKO Mice Causes Skin Xanthomas, Worsening of Inflammation, and Increased Coronary Atherosclerosis in the Absence of Hyperlipidemia.
Arterioscler Thromb Vasc Biol
; 42(7): 839-856, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35587694
3.
PLXNA1 and PLXNA3 cooperate to pattern the nasal axons that guide gonadotropin-releasing hormone neurons.
Development
; 146(21)2019 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31690636
4.
LAM Cells as Potential Drivers of Senescence in Lymphangioleiomyomatosis Microenvironment.
Int J Mol Sci
; 23(13)2022 Jun 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35806041
5.
A Novel SEMA3G Mutation in Two Siblings Affected by Syndromic GnRH Deficiency.
Neuroendocrinology
; 111(5): 421-441, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-32365351
6.
The Differential Roles for Neurodevelopmental and Neuroendocrine Genes in Shaping GnRH Neuron Physiology and Deficiency.
Int J Mol Sci
; 22(17)2021 Aug 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34502334
7.
Semaphorin Signaling in GnRH Neurons: From Development to Disease.
Neuroendocrinology
; 109(3): 193-199, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30504719
8.
Protein Kinase CK2 Subunits Differentially Perturb the Adhesion and Migration of GN11 Cells: A Model of Immature Migrating Neurons.
Int J Mol Sci
; 20(23)2019 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31779225
9.
Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency.
Dis Model Mech
; 16(3)2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36810932
10.
SEMA6A drives GnRH neuron-dependent puberty onset by tuning median eminence vascular permeability.
Nat Commun
; 14(1): 8097, 2023 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38062045
11.
T-cell lymphoblastic lymphoma shows differences and similarities with T-cell acute lymphoblastic leukemia by genomic and gene expression analyses.
Genes Chromosomes Cancer
; 50(12): 1063-75, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21987448
12.
Gonadotropin-releasing hormone-secreting neuron development and function: an update.
Minerva Endocrinol (Torino)
; 47(1): 58-69, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35103457
13.
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathies.
Front Cell Dev Biol
; 10: 979512, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36225316
14.
KMT2A: Umbrella Gene for Multiple Diseases.
Genes (Basel)
; 13(3)2022 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35328068
15.
Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum.
Genes (Basel)
; 12(7)2021 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34356091
16.
Semaphorin Regulation by the Chromatin Remodeler CHD7: An Emerging Genetic Interaction Shaping Neural Cells and Neural Crest in Development and Cancer.
Front Cell Dev Biol
; 9: 638674, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33869187
17.
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia.
J Clin Invest
; 131(24)2021 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34730112
18.
LGR4 deficiency results in delayed puberty through impaired Wnt/ß-catenin signaling.
JCI Insight
; 5(11)2020 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32493844
19.
In Vitro, Ex Vivo and In Vivo Techniques to Study Neuronal Migration in the Developing Cerebral Cortex.
Brain Sci
; 7(5)2017 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28448448
20.
Iron overload induces hypogonadism in male mice via extrahypothalamic mechanisms.
Mol Cell Endocrinol
; 454: 135-145, 2017 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28648620